Literature DB >> 24190543

Chronic treatment with olanzapine increases adiposity by changing fuel substrate and causes desensitization of the acute metabolic side effects.

Elodie M Girault1, Bruno Guigas, Anneke Alkemade, Ewout Foppen, Mariëtte T Ackermans, Susanne E la Fleur, Eric Fliers, Andries Kalsbeek.   

Abstract

Atypical antipsychotic drugs such as olanzapine induce weight gain and metabolic changes associated with the development of type 2 diabetes. The mechanisms underlying these metabolic side-effects are unknown at the moment. In this study, we investigated the metabolic changes induced by a chronic treatment, as well as the influence of a preceding chronic treatment on the acute effects of olanzapine on glucose metabolism. The effect of chronic olanzapine treatment (±6.5 mg/kg/day, administered via drinking water) on body weight, locomotor activity, body temperature, fat distribution and energy expenditure was investigated in male rats. After 5 weeks, the animals received an acute olanzapine challenge (intragastric, IG) at 3 mg/kg/h during 160 min to investigate the acute effects of olanzapine on glucose metabolism. Chronic olanzapine-treated animals showed a slight decrease in nocturnal body temperature, and increased perirenal fat pad weights as well as plasma leptin. In addition, chronic olanzapine-treated animals showed hyperinsulinaemia with unchanged blood glucose concentrations. The acute challenge with IG olanzapine elevated blood glucose levels and endogenous glucose production in control animals, but not in chronic olanzapine-pre-treated rats. Chronic olanzapine-treated animals also showed reduced locomotor activity and a higher respiratory exchange ratio. Thus, chronic treatment with olanzapine in rats causes desensitization to its acute effects on glucose metabolism but promotes adiposity probably due to a shift from lipids to carbohydrates as an energy source. Chronic exposure to olanzapine changes body fat distribution and insulin sensitivity in an unfavourable direction, but it is still unclear what the primary mechanism is.

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Year:  2013        PMID: 24190543     DOI: 10.1007/s00210-013-0933-5

Source DB:  PubMed          Journal:  Naunyn Schmiedebergs Arch Pharmacol        ISSN: 0028-1298            Impact factor:   3.000


  45 in total

1.  Factors influencing acute weight change in patients with schizophrenia treated with olanzapine, haloperidol, or risperidone.

Authors:  B R Basson; B J Kinon; C C Taylor; K A Szymanski; J A Gilmore; G D Tollefson
Journal:  J Clin Psychiatry       Date:  2001-04       Impact factor: 4.384

2.  Palatability, food intake and the behavioural satiety sequence in male rats.

Authors:  Y Ishii; J E Blundell; J C G Halford; R J Rodgers
Journal:  Physiol Behav       Date:  2003-10

3.  Neurobehavioral and metabolic long-term consequences of neonatal maternal deprivation stress and adolescent olanzapine treatment in male and female rats.

Authors:  Alvaro Llorente-Berzal; Virginia Mela; Erika Borcel; Manuel Valero; Meritxell López-Gallardo; Maria-Paz Viveros; Eva M Marco
Journal:  Neuropharmacology       Date:  2011-07-28       Impact factor: 5.250

4.  Negative effects of chronic oral chlorpromazine and olanzapine treatment on the performance of tasks designed to assess spatial learning and working memory in rats.

Authors:  A V Terry; S E Warner; L Vandenhuerk; A Pillai; S P Mahadik; G Zhang; M G Bartlett
Journal:  Neuroscience       Date:  2008-08-27       Impact factor: 3.590

5.  The quantification of gluconeogenesis in healthy men by (2)H2O and [2-(13)C]glycerol yields different results: rates of gluconeogenesis in healthy men measured with (2)H2O are higher than those measured with [2-(13)C]glycerol.

Authors:  M T Ackermans; A M Pereira Arias; P H Bisschop; E Endert; H P Sauerwein; J A Romijn
Journal:  J Clin Endocrinol Metab       Date:  2001-05       Impact factor: 5.958

6.  Atypical antipsychotic medications increase postprandial triglyceride and glucose levels in male rats: relationship with stearoyl-CoA desaturase activity.

Authors:  Robert K McNamara; Ronald Jandacek; Therese Rider; Patrick Tso; Allyson Cole-Strauss; Jack W Lipton
Journal:  Schizophr Res       Date:  2011-04-07       Impact factor: 4.939

7.  Olanzapine promotes fat accumulation in male rats by decreasing physical activity, repartitioning energy and increasing adipose tissue lipogenesis while impairing lipolysis.

Authors:  V L Albaugh; J G Judson; P She; C H Lang; K P Maresca; J L Joyal; C J Lynch
Journal:  Mol Psychiatry       Date:  2010-03-23       Impact factor: 15.992

8.  Insulin resistance and decreased glucose-stimulated insulin secretion after acute olanzapine administration.

Authors:  Araba F Chintoh; Steve W Mann; Loretta Lam; Carol Lam; Tony A Cohn; Paul J Fletcher; Jose N Nobrega; Adria Giacca; Gary Remington
Journal:  J Clin Psychopharmacol       Date:  2008-10       Impact factor: 3.153

Review 9.  Atypical antipsychotic-induced metabolic side effects: insights from receptor-binding profiles.

Authors:  H A Nasrallah
Journal:  Mol Psychiatry       Date:  2007-09-11       Impact factor: 15.992

10.  A double blind, placebo-controlled, randomized crossover study of the acute metabolic effects of olanzapine in healthy volunteers.

Authors:  Vance L Albaugh; Ravi Singareddy; David Mauger; Christopher J Lynch
Journal:  PLoS One       Date:  2011-08-09       Impact factor: 3.240

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  2 in total

1.  A comprehensive approach to predicting weight gain and therapy response in psychopharmacologically treated major depressed patients: A cohort study protocol.

Authors:  Maria S Simon; Barbara B Barton; Catherine Glocker; Richard Musil
Journal:  PLoS One       Date:  2022-07-21       Impact factor: 3.752

2.  The Wnt Signaling Pathway Effector TCF7L2 Mediates Olanzapine-Induced Weight Gain and Insulin Resistance.

Authors:  Ranran Li; Jianjun Ou; Li Li; Ye Yang; Jingping Zhao; Renrong Wu
Journal:  Front Pharmacol       Date:  2018-04-16       Impact factor: 5.810

  2 in total

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